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Ferrocene‐ and Biferrocene‐Containing Macrocycles towards Single‐Molecule Electronics

Cyclic multiredox centered systems are currently of great interest, with new compounds being reported and developments made in understanding their behavior. Efficient, elegant, and high‐yielding (for macrocyclic species) synthetic routes to two novel alkynyl‐conjugated multiple ferrocene‐ and biferr...

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Detalles Bibliográficos
Autores principales: Wilson, Lucy E., Hassenrück, Christopher, Winter, Rainer F., White, Andrew J. P., Albrecht, Tim, Long, Nicholas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499722/
https://www.ncbi.nlm.nih.gov/pubmed/28497507
http://dx.doi.org/10.1002/anie.201702006
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author Wilson, Lucy E.
Hassenrück, Christopher
Winter, Rainer F.
White, Andrew J. P.
Albrecht, Tim
Long, Nicholas J.
author_facet Wilson, Lucy E.
Hassenrück, Christopher
Winter, Rainer F.
White, Andrew J. P.
Albrecht, Tim
Long, Nicholas J.
author_sort Wilson, Lucy E.
collection PubMed
description Cyclic multiredox centered systems are currently of great interest, with new compounds being reported and developments made in understanding their behavior. Efficient, elegant, and high‐yielding (for macrocyclic species) synthetic routes to two novel alkynyl‐conjugated multiple ferrocene‐ and biferrocene‐containing cyclic compounds are presented. The electronic interactions between the individual ferrocene units have been investigated through electrochemistry, spectroelectrochemistry, density functional theory (DFT), and crystallography to understand the effect of cyclization on the electronic properties and structure.
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spelling pubmed-54997222017-07-21 Ferrocene‐ and Biferrocene‐Containing Macrocycles towards Single‐Molecule Electronics Wilson, Lucy E. Hassenrück, Christopher Winter, Rainer F. White, Andrew J. P. Albrecht, Tim Long, Nicholas J. Angew Chem Int Ed Engl Communications Cyclic multiredox centered systems are currently of great interest, with new compounds being reported and developments made in understanding their behavior. Efficient, elegant, and high‐yielding (for macrocyclic species) synthetic routes to two novel alkynyl‐conjugated multiple ferrocene‐ and biferrocene‐containing cyclic compounds are presented. The electronic interactions between the individual ferrocene units have been investigated through electrochemistry, spectroelectrochemistry, density functional theory (DFT), and crystallography to understand the effect of cyclization on the electronic properties and structure. John Wiley and Sons Inc. 2017-05-12 2017-06-06 /pmc/articles/PMC5499722/ /pubmed/28497507 http://dx.doi.org/10.1002/anie.201702006 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Wilson, Lucy E.
Hassenrück, Christopher
Winter, Rainer F.
White, Andrew J. P.
Albrecht, Tim
Long, Nicholas J.
Ferrocene‐ and Biferrocene‐Containing Macrocycles towards Single‐Molecule Electronics
title Ferrocene‐ and Biferrocene‐Containing Macrocycles towards Single‐Molecule Electronics
title_full Ferrocene‐ and Biferrocene‐Containing Macrocycles towards Single‐Molecule Electronics
title_fullStr Ferrocene‐ and Biferrocene‐Containing Macrocycles towards Single‐Molecule Electronics
title_full_unstemmed Ferrocene‐ and Biferrocene‐Containing Macrocycles towards Single‐Molecule Electronics
title_short Ferrocene‐ and Biferrocene‐Containing Macrocycles towards Single‐Molecule Electronics
title_sort ferrocene‐ and biferrocene‐containing macrocycles towards single‐molecule electronics
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499722/
https://www.ncbi.nlm.nih.gov/pubmed/28497507
http://dx.doi.org/10.1002/anie.201702006
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